to determine the prevalence and significance of chronic nephrotoxic effects of cisplatin therapy by 1) identifying patients with chronic cisplatin nephrotoxicity and 2) reviewing their QoL. Eventually, this could improve care in these patients
ID
Source
Brief title
Condition
- Nephropathies
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
number of patients with chronic cisplatin nephropathy (chronic kidney injury
defined as a reduced GFR or biochemical signs of tubulopathy).
Secondary outcome
Quality of life in patients with nephropathy versus no signs of nephropathy
Background summary
Cisplatin is the most widely used agent in the chemotherapy of cancer. The
chief limit to efficacy is its toxicity (nephrotoxicity, neurotoxicity and
ototoxicity). Cisplatin-induced nephropathy or chronic kidney injury can
present as a decreased glomerular filtration rate (GFR), and tubulopathy
leading to the loss of electrolytes such as magnesium. Most reports have
studied the short term effects of cisplatin therapy only (acute kidney injury
and initial hypomagnesemia). The long term nephrotoxic effects of cisplatin
however could be very relevant as chronic hypophosphatemia, hypomagnesemia and
a decreased GFR result in a decreased quality of life and increased mortality.
The timely diagnosis and therefore treatment of chronic cisplatin nephrotoxicty
could improve quality of life, morbidity and mortality of patients who have
been treated with cisplatin.
Study objective
to determine the prevalence and significance of chronic nephrotoxic effects of
cisplatin therapy by 1) identifying patients with chronic cisplatin
nephrotoxicity and 2) reviewing their QoL. Eventually, this could improve care
in these patients
Study design
cross-sectional study in which all patients who received cisplatin therapy more
than one year ago and visit the outpatient oncology clinic will be included.
Blood and urine investigations will be performed and a quality of life
questionnaire is taken after the patient has given his/her informed consent.
Study burden and risks
There is only a small risk accompanying the withdrawal of blood in those
patients in whom otherwise blood was not taken.
Geert Grooteplein Zuid 8
Nijmegen 6500 HB
NL
Geert Grooteplein Zuid 8
Nijmegen 6500 HB
NL
Listed location countries
Age
Inclusion criteria
age * 18 years old
last gift cisplatin more than 1 year ago
all doses of cisplatin
all original oncological diagnoses
Exclusion criteria
none
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL57381.091.16 |